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Identification
Molecular formula
C11H13NS2
CAS number
not available
IUPAC name
1-allylsulfanyl-N-benzyl-methanimidothioic acid
State
State

The compound is typically a solid at room temperature based on its molecular structure and molar mass.

Melting point (Celsius)
120.00
Melting point (Kelvin)
393.00
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.00
General information
Molecular weight
237.40g/mol
Molar mass
237.4000g/mol
Density
1.2000g/cm3
Appearence

Data on the appearance of this compound is not specifically known. Given the structural features, it may appear as a powder or crystalline solid.

Comment on solubility

Solubility of 1-allylsulfanyl-N-benzyl-methanimidothioic acid

The solubility of 1-allylsulfanyl-N-benzyl-methanimidothioic acid can be quite complex due to its unique chemical structure. Here are some key points to consider:

  • Polarity: The polar functional groups present in the molecule suggest that the compound may be partially soluble in polar solvents, such as water.
  • Solvent Effects: It is often beneficial to test solubility in different solvents. Common solvents (like ethanol, methanol, or dimethyl sulfoxide) may enhance solubility due to their ability to interact with polar functionalities.
  • Temperature Influence: Solubility might improve with an increase in temperature, which is a common trend in organic compounds.
  • pH Dependency: The acidic nature of the compound suggests that its solubility could greatly vary with changes in pH, potentially increasing in more basic environments.

In summary, while 1-allylsulfanyl-N-benzyl-methanimidothioic acid may exhibit limited solubility in water, its behavior in organic solvents and under varying conditions offers a plethora of avenues for exploration. Conducting empirical solubility tests remains paramount for a more definitive understanding.

Interesting facts

Interesting Facts about 1-Allylsulfanyl-N-benzyl-methanimidothioic Acid

1-Allylsulfanyl-N-benzyl-methanimidothioic acid is a fascinating compound that belongs to the class of thioic acids. It exhibits a range of intriguing features that are worth exploring:

  • Diverse Applications: This compound has potential applications in organic synthesis, particularly in the creation of various sulfur-containing moieties.
  • Structural Complexity: The structure showcases a unique blend of functionalities, combining an allyl group with sulfur and a methanimidothioic acid moiety, providing insights into the relationship between structure and reactivity.
  • Biological Relevance: Compounds with similar structures have been studied for their biological activities, including anti-cancer and anti-inflammatory properties, making 1-allylsulfanyl-N-benzyl-methanimidothioic acid an interesting subject for pharmacological research.
  • Synthetic Versatility: Its unique functional groups open pathways for potential modifications, which can lead to a variety of derivatives, each with differing chemical properties.
  • Reactivity of Thioic Acids: Thioic acids often display high reactivity due to the presence of the thiol group, which can readily participate in nucleophilic reactions, offering a rich area for synthetic chemists to explore.

In summary, the study of 1-allylsulfanyl-N-benzyl-methanimidothioic acid offers a glimpse into the fascinating world of organic sulfur compounds. As the field of chemistry continues to advance, the potential for discovering new applications and properties related to this compound remains vast. As scientific inquiry deepens, it may well lead to novel solutions in various domains, from pharmaceuticals to materials science.